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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362633Generated: October 30, 2026

Bicarbonate Ion → HCID 67003360, compound

https://huagongshe.com/reaction/2362633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicarbonate IonHCID 769—
Reactant4-((Morpholino)methyl)phenylboronic acid pinacol esterHCID 2795502—
ReactantHCID 67003856HCID 67003856—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
ProductHCID 67003360HCID 67003360—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred ambient solution of 5-(5-chloro-2-iodo-1-tosyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-2-(3-(4-methoxybenzyloxy)oxetan-3-yl)thiazole (Example 11G) (200 mg, 0.282 mmol) and 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)morpholine (120 mg, 0.395 mmol) in N,N-dimethylformamide (2.65 mL) was added saturated aqueous bicarbonate solution (0.883 mL) followed by bis(triphenylphosphine)palladium dichloride (13.88 mg, 0.020 mmol). The mixture was heated to 70° C. for 4 hours and was then quenched by the addition of water and ethyl acetate. The layers were separated, and the aqueous layer was extracted with additional ethyl acetate. The combined organics were dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel, eluting with a gradient of 0 to 30% ethyl acetate in hexane, to afford the title compound. MS ESI(+) m/z 757.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691810B2
Source datasetuspto-grants-2014_04
ORD IDord-f79ad057e24345228d187ad90dfac5ba
Source noteuspto-grants-2014_04